4-Iodobenzoyl chloride → 2-(4-Iodophenyl)-5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridine

HRID 1177571Notes

Reaction equation

HRID 1177571 reaction equation
[NH2:1][C:2]1[C:3](=[S:17])[NH:4][C:5]([C:8]2([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)[CH2:10][CH2:9]2)=[CH:6][CH:7]=1.[I:18][C:19]1[CH:27]=[CH:26][C:22]([C:23](Cl)=O)=[CH:21][CH:20]=1.NC1C(=S)NC=CC=1>>[I:18][C:19]1[CH:27]=[CH:26][C:22]([C:23]2[S:17][C:3]3[C:2]([N:1]=2)=[CH:7][CH:6]=[C:5]([C:8]2([C:11]4[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=4)[CH2:10][CH2:9]2)[N:4]=3)=[CH:21][CH:20]=1

Participants

4

Reactant 3

HCID 743734-Iodobenzoyl chlorideHCID 54631813-Aminopyridine-2-thiolHCID 591748363-amino-6-(1-phenylcyclopropyl)pyridine-2(1H)-thione

Product 1

HCID 671116852-(4-Iodophenyl)-5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridine

Procedure

Reaction of 3-amino-6-(1-phenylcyclopropyl)pyridine-2(1H)-thione (503.8 mg, 2.079 mmol) and 4-iodobenzoyl chloride (554 mg, 2.079 mmol) according to Reference V and the general procedure for the condensation of 3-aminopyridine-2-thione with aryl acid chlorides gave 2-(4-iodophenyl)-5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridine as a white solid. MS (ESI) m/z: Calculated: 454.0; Observed: 454.9 (M++1).

Sources & evidence

ORD record
ord-fb084f4550a940238102846142c60451
Source dataset
uspto-grants-2010_11
Patent number
US07842685B2

Reaction notes

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