Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014417Generated: October 25, 2026

2-Amino-4-methoxybenzamide → 2-({2-chloro-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}amino)-4-(methyloxy)benzamide

https://huagongshe.com/reaction/1014417

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-methoxybenzamideHCID 14023002—
Reactant2,4-dichloro-7-tosyl-7H-pyrrolo[2,3-d]pyrimidineHCID 53486828—
Product2-({2-chloro-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}amino)-4-(methyloxy)benzamideHCID 8664418629%

Reaction Steps

Using General Protocol II and starting with 2,4-dichloro-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidine (4.0 g, 11.7 mmol) and 2-amino-4-(methyloxy)benzamide (4.5 g, 26.8 mmol), 2-({2-chloro-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}amino)-4-(methyloxy)benzamide was isolated as a yellow solid (0.1.58 g, 29% yield); 1H NMR (400 MHz, DMSO-d6) δ ppm 2.33 (s, 3 H), 4.28 (s, 3 H), 6.62 (t, J=3.48 Hz, 1 H), 6.68 (ddd, J=6.00, 2.88, 2.66 Hz, 1 H), 7.41-7.46 (m, 2 H), 7.64 (s, 1 H), 7.74 (t, J=3.48 Hz, 1 H), 7.81-7.87 (m, 1 H), 7.92-7.98 (m, 2 H), 8.22 (s, 1 H), 8.32 (t, J=2.66 Hz, 1 H), 13.13 (s, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981903B2
Source datasetuspto-grants-2011_07
ORD IDord-0d10695b5d0d48f1b2b65e7d5535e42a
Source noteuspto-grants-2011_07