Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25219Generated: October 25, 2026

2-Methylbutylamine → HCID 69635630, compound

https://huagongshe.com/reaction/25219

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylbutylamineHCID 7283—
Reactant3-({1-[Bis(4-chlorophenyl)methyl]azetidin-3-ylidene}methanesulfonylmethyl)benzoic acidHCID 69635678—
ProductHCID 69635630HCID 69635630—

Reaction Steps

The operation is carried out under the conditions described in Example 124 starting with 110 mg of activated 3-({1-[bis(4-chlorophenyl)methyl]azetidin-3-ylidene}methanesulfonylmethyl)benzoic acid on TFP resin (121 μM) and 0.023 cm3 of 2-methylbutylamine. 49 mg of 3-({1-[bis(4-chlorophenyl)methyl]azetidin-3-ylidene}methanesulfonylmethyl)-N-(2-methylbutyl)benzamide are thus obtained [1H NMR spectrum (400 MHz, (CD3)2SO-d6, δ in ppm): from 0.80 to 0.95 (mt, 6H), from 1.05 to 120 (mt, 1H), 1.41 (mt, 1H), 1.64 (mt, 1H), 2.98 (s, 3H), 3.06 (mt, 1H), 3.19 (mt, 1H), 3.81 (mt, 2H), 4.23 (mt, 2H), 4.79 (s, 1H), 7.36 (d, J=8 Hz, 4H), 7.46 (d, J=8 Hz, 4H), from 7.35 to 7.60 (mt, 2H), 7.84 (broad s, 1H), 7.87 (broad d, J=8 Hz, 1H), 8.49 (t, J=5.5 Hz, 1H)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858603B2
Source datasetuspto-grants-2005_02
ORD IDord-b2d15ff376ac4b799fe2ec73bc89771d
Source noteuspto-grants-2005_02