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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173033Generated: October 26, 2026

Isopropylamine → Racemic-(trans)-n-isopropyl-2-{4-[({4-isopropyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl}methyl)amino]phenyl}cyclopropanecarboxamide

https://huagongshe.com/reaction/1173033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropylamineHCID 6363—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantRacemic-(trans)-2-{4-[({4-isopropyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl}methyl)amino]phenyl}cyclopropanecarboxylic acidHCID 11202011—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductRacemic-(trans)-n-isopropyl-2-{4-[({4-isopropyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl}methyl)amino]phenyl}cyclopropanecarboxamideHCID 1175240722%

Reaction Steps

To a mixture of racemic-(trans)-2-{4-[({4-isopropyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl}methyl)amino]phenyl}cyclopropanecarboxylic acid (I-2n) (0.05 g, 0.11 mmol) in dichloromethane (3 mL) and DMF (1 mL) was added HATU (0.06 g, 0.16 mmol). The mixture was stirred for 15 min followed by addition of isopropylamine (0.01 g, 0.16 mmol). The solution stirred for 3 h after which the dichloromethane was removed via rotavap. Sat. NaHCO3 and ethyl acetate were added and the organic layer separated and washed with H2O, dried over MgSO4, filtered and concentrated. The resulting oil was triterated with Et2O and formed a white ppt which was filtered and dried under high vacuum to give the title compound as a white powder (0.01 g, 22%). 1H NMR (400 MHz, CDCl3) δ 7.99 (d, 8.3 Hz, 2H), 7.63 (d, J=8.2 Hz, 2H), 6.94 (d, J=8.4 Hz, 2H), 6.60 (d, J=8.5 Hz, 2H), 5.37 (d, J=7.9 Hz, 1H), 4.45 (s, 2H), 4.10-4.08 (m, 1H), 3.93 (s, 1H), 3.16-3.13 (m, 1H), 2.39-2.37 (m, 1H), 1.54-1.50 (m, 1H), 1.42-1.39 (m, 1H), 1.35 (d, J=6.8 Hz, 6H), 1.15-1.09 (m, 7H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834013B2
Source datasetuspto-grants-2010_11
ORD IDord-917d3439307743aa93ea060685d8d52b
Source noteuspto-grants-2010_11